Loading…

Statins and Cardiovascular Risk in Rheumatic Diseases

Chronic inflammatory rheumatic diseases are associated with an increased risk of cardiovascular (CV) atherosclerotic events. The inflammatory state, which is the hallmark of chronic rheumatic diseases, is the important driving force for accelerated atherogenesis. Since the control of traditional ris...

Full description

Saved in:
Bibliographic Details
Published in:International journal of immunopathology and pharmacology 2012-01, Vol.25 (1), p.25-30
Main Authors: Marasini, B., Massarotti, M.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Request full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c294t-fb944c374bd5c5a98de19121ee2876a567112cf8acbd6fd6535f6c9c8a1cd37c3
container_end_page 30
container_issue 1
container_start_page 25
container_title International journal of immunopathology and pharmacology
container_volume 25
creator Marasini, B.
Massarotti, M.
description Chronic inflammatory rheumatic diseases are associated with an increased risk of cardiovascular (CV) atherosclerotic events. The inflammatory state, which is the hallmark of chronic rheumatic diseases, is the important driving force for accelerated atherogenesis. Since the control of traditional risk factors alone is insufficient in reducing the risk, much attention has been directed towards the potential use of statins. Statins, a family of drugs that suppress cholesterol biosynthesis by inhibiting the hydroxymethyl glutaryl coenzyme A reductase, have been shown to significantly reduce CV-related morbidity and mortality. In addition to lower lipid levels, several non-lipid lowering pleiotropic effects, including anti-inflammatory and immunomodulatory activities, make statins potential therapeutic agents in chronic rheumatic diseases. However, lipid metabolism in chronic rheumatic diseases is complex, since inflammatory states can induce alterations in lipid levels and function, so that cholesterol target levels from general guidelines may not be adequate in chronic inflammatory rheumatic diseases. Larger trials are needed to refine the precise benefits and health-utility associated with this therapy.
doi_str_mv 10.1177/039463201202500104
format article
fullrecord <record><control><sourceid>proquest_AFRWT</sourceid><recordid>TN_cdi_proquest_miscellaneous_1002568260</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_039463201202500104</sage_id><sourcerecordid>1002568260</sourcerecordid><originalsourceid>FETCH-LOGICAL-c294t-fb944c374bd5c5a98de19121ee2876a567112cf8acbd6fd6535f6c9c8a1cd37c3</originalsourceid><addsrcrecordid>eNp90EtLw0AUBeBBFFtq_4ALydJN7LxnspRqVSgIVddhMjPR1Dzq3ETw3zuh1Y3g6m6-c-AehM4JviJEqQVmGZeMYkIxFRgTzI_QlGKhU8U0P0bTEaSjmKA5wBaPhnGhySma0BhRjPApEk-96asWEtO6ZGmCq7pPA3aoTUg2FbwnVZts3vzQRGWTmwq8AQ9n6KQ0Nfj54c7Qy-r2eXmfrh_vHpbX69TSjPdpWWScW6Z44YQVJtPOk4xQ4j3VShohFSHUltrYwsnSScFEKW1mtSHWMWXZDF3ue3eh-xg89HlTgfV1bVrfDZATHJ-XmkocKd1TGzqA4Mt8F6rGhK-I8nGx_O9iMXRx6B-KxrvfyM8-ESz2AMyrz7fdENr473-V3y9NcbM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1002568260</pqid></control><display><type>article</type><title>Statins and Cardiovascular Risk in Rheumatic Diseases</title><source>SAGE Open Access</source><creator>Marasini, B. ; Massarotti, M.</creator><creatorcontrib>Marasini, B. ; Massarotti, M.</creatorcontrib><description>Chronic inflammatory rheumatic diseases are associated with an increased risk of cardiovascular (CV) atherosclerotic events. The inflammatory state, which is the hallmark of chronic rheumatic diseases, is the important driving force for accelerated atherogenesis. Since the control of traditional risk factors alone is insufficient in reducing the risk, much attention has been directed towards the potential use of statins. Statins, a family of drugs that suppress cholesterol biosynthesis by inhibiting the hydroxymethyl glutaryl coenzyme A reductase, have been shown to significantly reduce CV-related morbidity and mortality. In addition to lower lipid levels, several non-lipid lowering pleiotropic effects, including anti-inflammatory and immunomodulatory activities, make statins potential therapeutic agents in chronic rheumatic diseases. However, lipid metabolism in chronic rheumatic diseases is complex, since inflammatory states can induce alterations in lipid levels and function, so that cholesterol target levels from general guidelines may not be adequate in chronic inflammatory rheumatic diseases. Larger trials are needed to refine the precise benefits and health-utility associated with this therapy.</description><identifier>ISSN: 0394-6320</identifier><identifier>EISSN: 2058-7384</identifier><identifier>DOI: 10.1177/039463201202500104</identifier><identifier>PMID: 22507314</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Cardiovascular Diseases - prevention &amp; control ; Chronic Disease ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use ; Lipid Metabolism ; Rheumatic Diseases - complications ; Rheumatic Diseases - drug therapy ; Rheumatic Diseases - metabolism</subject><ispartof>International journal of immunopathology and pharmacology, 2012-01, Vol.25 (1), p.25-30</ispartof><rights>2012 SAGE Publications</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c294t-fb944c374bd5c5a98de19121ee2876a567112cf8acbd6fd6535f6c9c8a1cd37c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/039463201202500104$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/039463201202500104$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21965,27852,27923,27924,44944,45332</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.1177/039463201202500104?utm_source=summon&amp;utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22507314$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marasini, B.</creatorcontrib><creatorcontrib>Massarotti, M.</creatorcontrib><title>Statins and Cardiovascular Risk in Rheumatic Diseases</title><title>International journal of immunopathology and pharmacology</title><addtitle>Int J Immunopathol Pharmacol</addtitle><description>Chronic inflammatory rheumatic diseases are associated with an increased risk of cardiovascular (CV) atherosclerotic events. The inflammatory state, which is the hallmark of chronic rheumatic diseases, is the important driving force for accelerated atherogenesis. Since the control of traditional risk factors alone is insufficient in reducing the risk, much attention has been directed towards the potential use of statins. Statins, a family of drugs that suppress cholesterol biosynthesis by inhibiting the hydroxymethyl glutaryl coenzyme A reductase, have been shown to significantly reduce CV-related morbidity and mortality. In addition to lower lipid levels, several non-lipid lowering pleiotropic effects, including anti-inflammatory and immunomodulatory activities, make statins potential therapeutic agents in chronic rheumatic diseases. However, lipid metabolism in chronic rheumatic diseases is complex, since inflammatory states can induce alterations in lipid levels and function, so that cholesterol target levels from general guidelines may not be adequate in chronic inflammatory rheumatic diseases. Larger trials are needed to refine the precise benefits and health-utility associated with this therapy.</description><subject>Cardiovascular Diseases - prevention &amp; control</subject><subject>Chronic Disease</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</subject><subject>Lipid Metabolism</subject><subject>Rheumatic Diseases - complications</subject><subject>Rheumatic Diseases - drug therapy</subject><subject>Rheumatic Diseases - metabolism</subject><issn>0394-6320</issn><issn>2058-7384</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp90EtLw0AUBeBBFFtq_4ALydJN7LxnspRqVSgIVddhMjPR1Dzq3ETw3zuh1Y3g6m6-c-AehM4JviJEqQVmGZeMYkIxFRgTzI_QlGKhU8U0P0bTEaSjmKA5wBaPhnGhySma0BhRjPApEk-96asWEtO6ZGmCq7pPA3aoTUg2FbwnVZts3vzQRGWTmwq8AQ9n6KQ0Nfj54c7Qy-r2eXmfrh_vHpbX69TSjPdpWWScW6Z44YQVJtPOk4xQ4j3VShohFSHUltrYwsnSScFEKW1mtSHWMWXZDF3ue3eh-xg89HlTgfV1bVrfDZATHJ-XmkocKd1TGzqA4Mt8F6rGhK-I8nGx_O9iMXRx6B-KxrvfyM8-ESz2AMyrz7fdENr473-V3y9NcbM</recordid><startdate>201201</startdate><enddate>201201</enddate><creator>Marasini, B.</creator><creator>Massarotti, M.</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201201</creationdate><title>Statins and Cardiovascular Risk in Rheumatic Diseases</title><author>Marasini, B. ; Massarotti, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c294t-fb944c374bd5c5a98de19121ee2876a567112cf8acbd6fd6535f6c9c8a1cd37c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Cardiovascular Diseases - prevention &amp; control</topic><topic>Chronic Disease</topic><topic>Humans</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</topic><topic>Lipid Metabolism</topic><topic>Rheumatic Diseases - complications</topic><topic>Rheumatic Diseases - drug therapy</topic><topic>Rheumatic Diseases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marasini, B.</creatorcontrib><creatorcontrib>Massarotti, M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of immunopathology and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Marasini, B.</au><au>Massarotti, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Statins and Cardiovascular Risk in Rheumatic Diseases</atitle><jtitle>International journal of immunopathology and pharmacology</jtitle><addtitle>Int J Immunopathol Pharmacol</addtitle><date>2012-01</date><risdate>2012</risdate><volume>25</volume><issue>1</issue><spage>25</spage><epage>30</epage><pages>25-30</pages><issn>0394-6320</issn><eissn>2058-7384</eissn><abstract>Chronic inflammatory rheumatic diseases are associated with an increased risk of cardiovascular (CV) atherosclerotic events. The inflammatory state, which is the hallmark of chronic rheumatic diseases, is the important driving force for accelerated atherogenesis. Since the control of traditional risk factors alone is insufficient in reducing the risk, much attention has been directed towards the potential use of statins. Statins, a family of drugs that suppress cholesterol biosynthesis by inhibiting the hydroxymethyl glutaryl coenzyme A reductase, have been shown to significantly reduce CV-related morbidity and mortality. In addition to lower lipid levels, several non-lipid lowering pleiotropic effects, including anti-inflammatory and immunomodulatory activities, make statins potential therapeutic agents in chronic rheumatic diseases. However, lipid metabolism in chronic rheumatic diseases is complex, since inflammatory states can induce alterations in lipid levels and function, so that cholesterol target levels from general guidelines may not be adequate in chronic inflammatory rheumatic diseases. Larger trials are needed to refine the precise benefits and health-utility associated with this therapy.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>22507314</pmid><doi>10.1177/039463201202500104</doi><tpages>6</tpages></addata></record>
fulltext fulltext_linktorsrc
identifier ISSN: 0394-6320
ispartof International journal of immunopathology and pharmacology, 2012-01, Vol.25 (1), p.25-30
issn 0394-6320
2058-7384
language eng
recordid cdi_proquest_miscellaneous_1002568260
source SAGE Open Access
subjects Cardiovascular Diseases - prevention & control
Chronic Disease
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects
Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use
Lipid Metabolism
Rheumatic Diseases - complications
Rheumatic Diseases - drug therapy
Rheumatic Diseases - metabolism
title Statins and Cardiovascular Risk in Rheumatic Diseases
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T22%3A55%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_AFRWT&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Statins%20and%20Cardiovascular%20Risk%20in%20Rheumatic%20Diseases&rft.jtitle=International%20journal%20of%20immunopathology%20and%20pharmacology&rft.au=Marasini,%20B.&rft.date=2012-01&rft.volume=25&rft.issue=1&rft.spage=25&rft.epage=30&rft.pages=25-30&rft.issn=0394-6320&rft.eissn=2058-7384&rft_id=info:doi/10.1177/039463201202500104&rft_dat=%3Cproquest_AFRWT%3E1002568260%3C/proquest_AFRWT%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c294t-fb944c374bd5c5a98de19121ee2876a567112cf8acbd6fd6535f6c9c8a1cd37c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1002568260&rft_id=info:pmid/22507314&rft_sage_id=10.1177_039463201202500104&rfr_iscdi=true